VITA CEREC SET AND VITA CEREC BLOCS
K-Number: K895901 · 1992-01-17
Advertisement
Device Summary
Frequently Asked Questions
What is the VITA CEREC SET AND VITA CEREC BLOCS?
VITA CEREC SET AND VITA CEREC BLOCS is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Vident. The 510(k) number is K895901.
When did VITA CEREC SET AND VITA CEREC BLOCS receive FDA 510(k) clearance?
VITA CEREC SET AND VITA CEREC BLOCS received FDA 510(k) clearance on 1992-01-17, under 510(k) number K895901.
Who is the listed applicant for VITA CEREC SET AND VITA CEREC BLOCS?
The FDA 510(k) record lists Vident as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITA CEREC SET AND VITA CEREC BLOCS?
The FDA product code for VITA CEREC SET AND VITA CEREC BLOCS is ELW.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Vident as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ELW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement